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This Sandbox is Reserved from January 10, 2010, through April 10, 2011 for use in BCMB 307-Proteins course taught by Andrea Gorrell at the University of Northern British Columbia, Prince George, BC, Canada.
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To get started:
- Click the edit this page tab at the top. Save the page after each step, then edit it again.
- Click the 3D button (when editing, above the wikitext box) to insert Jmol.
- show the Scene authoring tools, create a molecular scene, and save it. Copy the green link into the page.
- Add a description of your scene. Use the buttons above the wikitext box for bold, italics, links, headlines, etc.
More help: Help:Editing
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2fbv, resolution 2.40Å ()
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Ligands:
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Gene:
| WRN, RECQ3, RECQL2 (Homo sapiens)
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Related:
| 2fbt, 2fbx, 2fby, 2fc0
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Resources:
| FirstGlance, OCA, RCSB, PDBsum
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Coordinates:
| save as pdb, mmCIF, xml
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Werner (WRN) protein is one of the five human RecQDNA helicases, which unwinds DNA for translocation. WRN has a functional exonuclease domain.
WRN protein protects human from cancer; as well as, premature aging. When the gene coding for WRN is mutated a autosomal recessive disorder causing rapid aging(osteoporosis, atherosclerosis and cancer). This is known as Werner syndrome which appears at puberty.
Function
Structure
WRN is a enzyme with both magnesium and ATP-dependent DNA-helicase activity with a 3'->5' exonuclease
activity towards double-stranded DNA.
Magnesium
Crystallization
Active Site
Substrate-Binding Site
Reference